Entry |
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Symbol |
RPGRIP1
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Name |
X-linked retinitis pigmentosa GTPase regulator-interacting protein 1
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Disease |
H00481 | Cone-rod dystrophy and cone dystrophy |
H00837 | Leber congenital amaurosis |
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Brite |
KEGG Orthology (KO) [BR:ko00001]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins
K16512 RPGRIP1; X-linked retinitis pigmentosa GTPase regulator-interacting protein 1
Cilium and associated proteins [BR:ko03037]
Primary cilia and associated proteins
Other primary cilia associated proteins
K16512 RPGRIP1; X-linked retinitis pigmentosa GTPase regulator-interacting protein 1
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Genes |
» show all
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Reference |
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Authors |
Patil H, Tserentsoodol N, Saha A, Hao Y, Webb M, Ferreira PA |
Title |
Selective loss of RPGRIP1-dependent ciliary targeting of NPHP4, RPGR and SDCCAG8 underlies the degeneration of photoreceptor neurons. |
Journal |
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Sequence |
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Reference |
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Authors |
Zhao Y, Hong DH, Pawlyk B, Yue G, Adamian M, Grynberg M, Godzik A, Li T |
Title |
The retinitis pigmentosa GTPase regulator (RPGR)- interacting protein: subserving RPGR function and participating in disk morphogenesis. |
Journal |
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Sequence |
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LinkDB |
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